Natural history of six neonates with severe MTM1-related X-linked myotubular myopathy
Objective X-linked myotubular myopathy (XLMTM) caused by MTM1 gene variation is a rare neuromuscular disease. Currently, the systematic summary of the early natural history and diagnostic clinical characteristics of XLMTM patients in China is still incomplete. Methods We retrospectively reviewed cli...
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| Formatua: | Artigo |
| Hizkuntza: | Chinês |
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Editorial Office of Journal of Clinical Pediatrics
2026-02-01
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| Saila: | Linchuang erke zazhi |
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| Sarrera elektronikoa: | https://jcp.xinhuamed.com.cn/fileup/1000-3606/PDF/1770018652870-1358503444.pdf |
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